A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660213



Internal ID9926318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47610065..47614493hg38UCSC Ensembl
chr4:47612082..47616510hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg384429
hg194429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5590714, essv6016082
SamplesHG00699, NA18636
Known GenesCORIN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660213
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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